69796-19-6 Usage
Uses
Used in Pharmaceutical Synthesis:
1-(3,4-dichlorophenyl)-2-nitropropan-1-ol is used as an intermediate in the pharmaceutical industry for the synthesis of various pharmaceutical substances and organic compounds. Its unique chemical structure contributes to the development of new drugs and medications.
Used in Antimicrobial Applications:
In the field of microbiology, 1-(3,4-dichlorophenyl)-2-nitropropan-1-ol is utilized for its potent antimicrobial properties. It serves as an active ingredient in antiseptic and disinfectant products, helping to eliminate harmful microorganisms and maintain a clean and healthy environment.
Used in Cancer Treatment Research:
1-(3,4-dichlorophenyl)-2-nitropropan-1-ol is also being studied for its potential use in the treatment of certain types of cancer. Its effectiveness in targeting cancer cells and its antimicrobial properties make it a promising candidate for further research and development in oncology.
Check Digit Verification of cas no
The CAS Registry Mumber 69796-19-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,9,7,9 and 6 respectively; the second part has 2 digits, 1 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 69796-19:
(7*6)+(6*9)+(5*7)+(4*9)+(3*6)+(2*1)+(1*9)=196
196 % 10 = 6
So 69796-19-6 is a valid CAS Registry Number.
69796-19-6Relevant academic research and scientific papers
Catalytic asymmetric henry reaction of nitroalkanes and aldehydes catalyzed by a chiral N, N '-dioxide/Cu(I) complex
Mei, Hongjiang,Xiao, Xiao,Zhao, Xiaohu,Fang, Bing,Liu, Xiaohua,Lin, Lili,Feng, Xiaoming
, p. 2272 - 2280 (2015/03/18)
An easily available N,N'-dioxide/Cu(I) complex has been developed for the catalytic asymmetric nitroaldol (Henry) reaction of aldehydes with nitroethane. Under mild reaction conditions, a series of substituted aromatic, heteroaromatic and α,β-unsaturated
Enantioselective Henry reaction catalyzed by a copper(II) glucoBOX complex
Reddy, B.V.Subba,George, Jimil
experimental part, p. 1169 - 1175 (2011/10/17)
A highly enantioselective Henry reaction has been developed using a chiral copper(II)-glucoBOX complex. The catalytic system works well with a wide range of aromatic, aliphatic and heteroaromatic aldehydes to afford the corresponding nitroalkanols with hi
